Canonical Allele Identifier: CA1215986720
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811676_192811687delinsGACCTTGAATTC , CM000663.2:g.192811676_192811687delinsGACCTTGAATTC GRCh38
NC_000001.10:g.192780806_192780817delinsGACCTTGAATTC , CM000663.1:g.192780806_192780817delinsGACCTTGAATTC GRCh37
NC_000001.9:g.191047429_191047440delinsGACCTTGAATTC NCBI36
NG_012800.1:g.7638_7649delinsGACCTTGAATTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*80_*91delinsGACCTTGAATTC MANE Select ENSP00000235382.5:n.*80_*91delinsGACCTTGAATTC
ENST00000235382.6:c.*80_*91delinsGACCTTGAATTC ENSP00000235382.5:n.*80_*91delinsGACCTTGAATTC
NM_002923.3:c.*80_*91delinsGACCTTGAATTC NP_002914.1:n.*80_*91delinsGACCTTGAATTC
NM_002923.4:c.*80_*91delinsGACCTTGAATTC MANE Select NP_002914.1:n.*80_*91delinsGACCTTGAATTC